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Peer-reviewed veterinary case report

Miniplasmin dissolves femoral artery clots in dogs

By Fu, Jieying et al.·Published in Thrombosis research·2008·Department of Pharmacology and Toxicology, China·View original on PubMed

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Original publication title: The thrombolytic effect of miniplasmin in a canine model of femoral artery thrombosis.

Species:
dog

Plain-English summary

A group of dogs with blocked femoral arteries due to blood clots were treated with a new drug called miniplasmin to see if it could safely dissolve the clots. The dogs received different doses of miniplasmin, and the results showed that it quickly restored blood flow without causing bleeding complications, unlike a standard treatment called rt-PA, which had a higher risk of bleeding. All dogs treated with the higher doses of miniplasmin had successful blood flow restoration, and none experienced re-blockage. This suggests that miniplasmin could be a promising option for treating blood clots in dogs.

People also search for: dog blood clot treatment · femoral artery blockage in dogs · miniplasmin for dogs

Abstract

BACKGROUND AND PURPOSE: Miniplasmin was a des-kringle variant of plasminogen with potential pharmacological application. We investigated the thrombolytic effect of miniplasmin in a canine model of femoral artery thrombosis. METHODS: In anesthetized dogs, a stable occlusive thrombus was formed by mechanical and electrolytic injury of the vessel wall, that the animals were later injected with miniplasmin (0.75 mg/kg, 1.5 mg/kg and 3.0 mg/kg, i.a.) and rt-PA (0.5 mg/kg, i.a.) intra-arterially. Hemodynamic parameters and hemorrhage status were monitored for 2 h. Thrombin time, activated partial thromboplastin time, prothrombin time and fibrinogen concentration were tested at 2 h after administration. Fibrin degradation product and D-dimer concentration were tested by ELISA. RESULTS: The incidence of reperfusion in the miniplasmin (3.0 and 1.5 mg/kg) groups was 100%, and time to reperfusion was (3.3+/-1.0) and (7.0+/-2.3) min, which was shorter than rt-PA. After reperfusion, none of the vessels in the miniplasmin (1.5 and 3.0 mg/kg) groups reoccluded, whereas 20% of vessels reoccluded in the rt-PA group. Rudimental thrombus mass in the miniplasmin (1.5 and 3.0 mg/kg) groups were smaller than rt-PA. The operative wounds in all miniplasmin groups had no hemorrhage within 2 h. There were no significant differences in thrombin time, activated partial thromboplastin time and prothrombin time. Fibrinogen concentration in the miniplasmin (3.0 mg/kg) group reduced significantly as compared with baseline and thrombosis values, whereas these values in the miniplasmin (1.5 and 0.75 mg/kg) groups were unchanged. Fibrin degradation product and D-dimer concentration increased significantly after thrombolysis. CONCLUSIONS: The results suggest that miniplasmin may be useful for the treatment of thrombosis and without complication of hemorrhage. This is in contrast to rt-PA, which intrinsically has a higher risk of occurring the hemorrhage risk.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/18328540/